Tert-Butyldimethyl((2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Allyl)Oxy)Silane
97%
- Product Code: 243689
CAS:
350498-98-5
| Molecular Weight: | 298.3 g./mol | Molecular Formula: | C₁₅H₃₁BO₃Si |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a bifunctional coupling agent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The compound contains both a boronate ester and a silyl-protected allyl alcohol moiety, enabling sequential or selective transformations. It serves as a versatile building block for introducing allyl functionalities in complex molecule synthesis, especially in pharmaceuticals and agrochemicals. The silyl ether group provides stability and chemoselectivity during reaction sequences, while the boronate group allows for palladium-catalyzed carbon-carbon bond formation. Commonly applied in the synthesis of bioactive molecules and functional materials where controlled reactivity and orthogonal protection are required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,980.00 |
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| 0.250 | 10-20 days | ฿11,700.00 |
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| 1.000 | 10-20 days | ฿24,620.00 |
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Tert-Butyldimethyl((2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Allyl)Oxy)Silane
Used as a bifunctional coupling agent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The compound contains both a boronate ester and a silyl-protected allyl alcohol moiety, enabling sequential or selective transformations. It serves as a versatile building block for introducing allyl functionalities in complex molecule synthesis, especially in pharmaceuticals and agrochemicals. The silyl ether group provides stability and chemoselectivity during reaction sequences, while the boronate group allows for palladium-catalyzed carbon-carbon bond formation. Commonly applied in the synthesis of bioactive molecules and functional materials where controlled reactivity and orthogonal protection are required.
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